{"title":"3-(5-甲酰基-3-硫氧基- 3h -[1,2]二硫醇-4-基)丙酸的制备","authors":"M. Chollet-Krugler, J. Burgot","doi":"10.1080/02786110310001625052","DOIUrl":null,"url":null,"abstract":"3-(5-Formyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid has been obtained from 3-[5-(hydroxyiminomethyl)-3-thioxo-3H-[1,2]dithiol-4-yl]propionic acid under standard conditions. Conversely, for the hydroxyimino derivative the general procedure failed and so it has been prepared by the action, in a basic medium, of isoamyl nitrite on 3-(5-methyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid ethyl ester.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":"8 1","pages":"195 - 199"},"PeriodicalIF":0.0000,"publicationDate":"2003-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"On the preparation of 3-(5-Formyl-3-thioxo-3H-[1,2]dithiol-4-yl)-propionic acid\",\"authors\":\"M. Chollet-Krugler, J. Burgot\",\"doi\":\"10.1080/02786110310001625052\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"3-(5-Formyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid has been obtained from 3-[5-(hydroxyiminomethyl)-3-thioxo-3H-[1,2]dithiol-4-yl]propionic acid under standard conditions. Conversely, for the hydroxyimino derivative the general procedure failed and so it has been prepared by the action, in a basic medium, of isoamyl nitrite on 3-(5-methyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid ethyl ester.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":\"8 1\",\"pages\":\"195 - 199\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02786110310001625052\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sulfur Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/02786110310001625052","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
On the preparation of 3-(5-Formyl-3-thioxo-3H-[1,2]dithiol-4-yl)-propionic acid
3-(5-Formyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid has been obtained from 3-[5-(hydroxyiminomethyl)-3-thioxo-3H-[1,2]dithiol-4-yl]propionic acid under standard conditions. Conversely, for the hydroxyimino derivative the general procedure failed and so it has been prepared by the action, in a basic medium, of isoamyl nitrite on 3-(5-methyl-3-thioxo-3H-[1,2]dithiol-4-yl)propionic acid ethyl ester.
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